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Methods for the regulation of the prostaglandin f synthase (PGFS) activity of akr1b1 and uses thereof

a technology of prostaglandin f synthase and akr1b1, which is applied in the field of methods for the regulation of the prostaglandin f synthase (pgfs) activity of akr1b1, can solve the problems of inability to fully realize the effect of pgfs

Inactive Publication Date: 2013-12-05
UNIV LAVAL
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, in diabetic hyperglycemia, the cells undergoing insulin-independent uptake of glucose are producing significant quantities of sorbitol.
This leads to an accumulation of sorbitol in the cells because of the poor penetration of sorbitol across cellular membrane and its slow metabolism by sorbitol dehydrogenase.
However, AKR1B1 inhibitors developed by pharmaceutical companies, such as Tolrestat™, Statil™ and Zopolrestat™, and which are administered for blocking the reduction of glucose into sorbitol in diabetic subjects having neuropathies, have often been found to be associated with undesirable hepatic side-effects (FIG. 2).
However, under special conditions such as insulin resistance, diabetes, oxidative stress or COX inhibitor therapy, these intrinsic feedback mechanisms can become impaired or inoperative.
Overproduction of PGF2α relative to PGE2 could therefore occur in such conditions, which could lead to ischemia for example.
Underproduction of PGF2α relative to PGE2 could also occur, for example in the eye, which could ultimately result in an increased ocular pressure.
Moreover, following the approval of inhaled insulin for the treatment of diabetes, it was found that absorption was limited by the constriction of bronchi, an effect that could be potentiated by PGF2α.

Method used

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  • Methods for the regulation of the prostaglandin f synthase (PGFS) activity of akr1b1 and uses thereof
  • Methods for the regulation of the prostaglandin f synthase (PGFS) activity of akr1b1 and uses thereof
  • Methods for the regulation of the prostaglandin f synthase (PGFS) activity of akr1b1 and uses thereof

Examples

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example 1

The Human AKR1B1 Qualifies as a Functional PGFS in the Endometrium

[0116]In the bovine endometrium, we previously demonstrated a strong PGFS activity of AKR1B5 recently renamed as bos taurus AKR1B1 (Gene ID: 317748), a new function for this enzyme previously known for its 20α-HSD and glucose metabolism activities (Madore et al., J Biol Chem 278(13); 11205-12, 2003). The human and bovine AKR1B1 both belong to the aldoketoreductase 1B family and share 86% identity or homology. The human AKR1B1 (Gene ID: 231) also known as the aldose reductase is highly expressed in the placenta for glucose metabolism and in the eye and kidney for osmotic regulation.

[0117]After identifying the bovine AKR1B1 as a functional PGFS, we have found that AKR1B1 expression was associated with PGF2α production in human endometrial cell lines and in decidualized stromal cells (Chapdelaine et al., Mol Hum Reprod, 12(5); 309-19, 2006). However, expression of AKR1B1 within the human endometrium and its ability to ac...

example 2

Retrovirus Infection and Establishment of SV40 Tag Cell Lines Expressing PGFS Activity

[0140]The retroviral vector SSR69 containing SV40 large TAG and a gene resistant to hygromycin was transfected with Effectene™ (Qiagen, Mississauga, ON, Canada) in the mouse amphotropic packaging cell line PA 317. The resulting colonies resistant to hygromycin (800 μg / ml, Roche, Mississauga, ON, Canada) were cultured, and the supernatants containing amphotropic viruses were collected and used to infect, separately, purified stromal and epithelial cells in primary culture. Endometrial cells grown in six-well plates were infected in the presence of polybrene (8μg / ml, Sigma) for 6 h, and the procedure was repeated 24 h later. The day following the last infection, the cells were trypsinized and seeded in 10 mm dishes in the presence of hygromycin (400 μg / ml). The cultures were grown for 7-8 days until the TAG-infected cells formed colonies while control non-infected cells died in the presence of the an...

example 3

Establishment of a Link Between AKR1B1 and Cox-2-Inhibitor-Associated Increased Risk of Heart Failure

[0143]Following the discovery of AKR1B1 as a major PGFS involved in the synthesis of PGF2α, and since AKR1B1 has been involved in diabetes-associated pathologies, and that its impact on cardiac and cerebral ischemia has been demonstrated in transgenic mice (Hwang Y. C. et al., 2004; Iwata K. et al., 2006; Vikramadithyan RK), we investigated if the PGFS function of AKR1B1 could allow for the identification of PGF2α as a molecule responsible for ischemia and pain.

[0144]The PGFS activity of AKR1B1 therefore represents a crucial step in the synthesis of PGF2α from PGH2 released by COX-1 and COX-2. The COX-inhibiting NSAIDs are commonly used in the treatment of headaches and muscle aches. Prior art studies of AKR1B1 mainly focused on its role in polyols synthesis or in lipid detoxification. While AKR1B1 inhibitors have been developed to treat pathological conditions such as diabetic compl...

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Abstract

AKR1B1 (EC 1.1.1.21) is an aldose reductase that has mainly been associated with the polyol pathway, and more recently with lipid deperoxidation. We have discovered that the primary activity of this enzyme is rather a PGFS activity, catalyzing the transformation of PGH2 into PGF2α. AKR1B1 as a therapeutic target, and method for modulating its expression and activity are provided. Methods for regulating the expression and activity of PGF2α are also provided.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS[0001]The present application is a divisional of co-pending U.S. application Ser. No. 12 / 743,206, filed May 9, 2011, which is a national stage of PCT / CA2008 / 002012, filed Nov. 14, 2008, and claims priority benefit of U.S. Provisional Application No. 60 / 988,220, filed Nov. 15, 2007. The applications are incorporated by reference herein in their entirety.FIELD OF THE INVENTION[0002]The present invention relates to a method for modulating and monitoring PGF2α levels and activity in a subject in need thereof by modulating AKR1B1 (aldose reductase) levels or its PGFS activity in the subject. AKR1B1 as a therapeutic target, and method for modulating its expression and PGFS activity are provided.BACKGROUND OF THE INVENTION[0003]Prostanoids, such as prostaglandins (PGs), thromboxanes (TXs) and prostacyclin (PGI2), are lipid compounds enzymatically derived from free fatty acids (FFAs). All prostanoids contain 20 carbon with a 5-carbon ring. Based on the...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K31/517A61K31/197A61K31/4188A61K31/501A61K31/426C12N5/071C12N5/077C12N15/113
CPCA61K31/517A61K31/501A61K31/426A61K31/4188A61K31/197A61K31/713C12N15/1137C12N2310/14C12N2503/02C12Q1/26C12Y101/01188G01N33/88G01N2333/902G01N2500/10G01N2800/52A61P11/08A61P15/00A61P3/00A61P9/10
Inventor FORTIER, MICHAELCHAPDELAINE, PIERREBRESSON, EVAMADORE, ERIC
Owner UNIV LAVAL
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